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Three different causes of hypercalciuria
S Skalova1, M Konrad, S Kutilek
1Pediatrics, Faculty of Medicine in Hradec Kralove, Charles University in Prague, Hradec Kralove, Czech Republic.
Insights
Hypercalciuria, or high urinary calcium, presents with symptoms like kidney stones and pain. Early assessment is crucial for children with these signs to diagnose conditions like idiopathic hypercalciuria or bone disease.
Area of Science:
- Pediatric Nephrology
- Clinical Medicine
- Biochemistry
Background:
- Hypercalciuria is defined by elevated urinary calcium excretion (≥0.1 mmol/kg/24h).
- It can stem from diverse underlying medical conditions.
- Common clinical manifestations include hematuria, abdominal pain, and urolithiasis.
Observation:
- Presents three pediatric case reports of hypercalciuria with distinct etiologies.
- Diagnoses included idiopathic hypercalciuria, familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and metabolic bone disease of prematurity.
- Highlights the varied origins of hypercalciuria in children.
Findings:
- Emphasizes the critical role of assessing hypercalciuria in pediatric cases.
- Essential for children presenting with urolithiasis, nephrocalcinosis, or bone demineralization.
- Recommends including hypercalciuria evaluation in the differential diagnosis for hematuria, recurrent abdominal pain, UTIs, and enuresis.
Implications:
- Early detection and diagnosis of hypercalciuria are vital for appropriate management.
- Guides pediatricians in diagnosing complex cases presenting with non-specific symptoms.
- Underscores the importance of a comprehensive diagnostic approach in pediatric nephrology.
Abstract:
Hypercalciuria is defined as urinary calcium excretion ≥0.1 mmol/kg/24 h, and can be a result of various disease states. The most frequent clinical signs of hypercalciuria include hematuria, abdominal pain, urolithiasis, nephrocalcinosis, dysuria, enuresis, and urinary tract infection. 3 case reports of children with hypercalciuria of different origin are presented, with final diagnoses of (1)idiopathic hypercalciuria, (2)familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and (3)metabolic bone disease of prematurity, respectively. Assessment of hypercalciuria is essential in all children with urolithiasis and nephrocalcinosis, or demineralization of bone. It should be also a part of differential diagnostic procedure in hematuria, recurrent abdominal pain, urinary tract infection and enuresis in childhood.
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